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[Mitochondrial antioxidant SkQl decreases intensity of ventricular arrhythmias caused by epinephrine]
Abstract:
Preventive action of new antioxidant SkQ1 has been studied in rats on model of cardiac arrhythmia caused by epinephrine. The SkQ1 substance was given in dosages from 0.02 up to 20 moles/kg per os 2 weeks prior to experiment. Intravenous bolus introduction of epinephrine (10 or 6 mkg/kg in different experimental series) caused an immediate rise of arterial pressure in average by 19% and decrease in heart rate in average by 44%. The degree of changes of these parameters was approximately identical in all groups. Arrhythmia in the form of ventricular extrasystolia arose in the first 5 min. The total number of extrasystoles, and index of arrhythmia intensity have been 2-3 times lower in rats receiding SkQ1 in doses of 0.5, 2 and 20 moles/kg. It was combined with increased survival rate of animals. Smaller dosages of SkQ1 (0.02-0.1 moles/kg) were ineffective. Results have shown that administration of mitochondrial antioxidant SkQ1 raises stability of the myocardium to arrhythmogenic action of epinephrine.
Insights
New antioxidant SkQ1 protected rats against epinephrine-induced cardiac arrhythmia. Effective doses of SkQ1 (mitochondrial antioxidant) significantly reduced extrasystoles and improved survival rates in rats.
Area of Science:
- Cardiovascular Pharmacology
- Mitochondrial Antioxidants
- Cardiac Electrophysiology
Context:
- Cardiac arrhythmia is a significant health concern.
- Epinephrine is known to induce cardiac arrhythmias.
- Mitochondrial dysfunction plays a role in cardiac pathology.
Purpose:
- To investigate the preventive effects of the novel antioxidant SkQ1 on epinephrine-induced cardiac arrhythmia in a rat model.
- To determine the effective dosage range of SkQ1 for cardioprotection.
Summary:
- Rats were pre-treated with varying doses of SkQ1 (0.02-20 µmol/kg) for two weeks before epinephrine administration.
- Epinephrine induced significant cardiac arrhythmia, characterized by ventricular extrasystoles.
- SkQ1 administration at doses of 0.5, 2, and 20 µmol/kg reduced arrhythmia intensity by 2-3 times and increased survival rates.
- Lower doses of SkQ1 (0.02-0.1 µmol/kg) showed no protective effect.
Impact:
- Mitochondrial antioxidant SkQ1 demonstrates significant cardioprotective effects against arrhythmogenic stimuli.
- SkQ1 enhances myocardial stability, offering a potential therapeutic strategy for preventing cardiac arrhythmias.
- These findings highlight the therapeutic potential of targeting mitochondrial function in cardiovascular disease.
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